CH181249A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH181249A CH181249A CH181249DA CH181249A CH 181249 A CH181249 A CH 181249A CH 181249D A CH181249D A CH 181249DA CH 181249 A CH181249 A CH 181249A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- amino
- preparation
- red
- clear
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoifes. Es wurde gefunden, dass man einen wert vollen Azofarbstoff erhält, wenn man die Diazoverbindung von 1-Amino-2-ohlor-4-nitro- benzol mit (N-Äthyl-N-phenyl-)-ss-amino-pro- pionsäurenitril kuppelt.
Der neue Azofarbstoff eignet sich vor züglich zum Färben von Celluloseestern und -äthern, die er in sehr klaren, leuchtend scharlachroten Tönen färbt, ferner zur Her stellung gefärbter Firnisse, Spiritus- oder Nitrocelluloselacke, die damit klare rote Überzüge geben; Stearin, Paraffin, Fette und Öle werden gelbrot gefärbt.
<I>Beispiel:</I> 173 Teile 1-Amino-2-chlor-4-nitrobenzol werden diazotiert und mit einer Lösung von 180 Teilen (N-Äthyl-N-phenyl)-p-amino-pro- pion-säure-nitril in 250 Teilen konzentrierter Salzsäure und 2000 Teilen Wasser unter Zusatz von soviel Natriumacetat gekuppelt dass die Lösung nicht mehr mineralsauer ist. Die Kupplung ist nach kurzer Zeit beendet.
Process for the production of an azo dye. It has been found that a valuable azo dye is obtained if the diazo compound of 1-amino-2-chloro-4-nitrobenzene is coupled with (N-ethyl-N-phenyl) -s-amino-propionic acid nitrile .
The new azo dye is particularly suitable for dyeing cellulose esters and ethers, which it dyes in very clear, bright scarlet shades, and also for producing colored varnishes, spirit or nitrocellulose varnishes, which give them clear red coatings; Stearin, paraffin, fats and oils are colored yellow-red.
<I> Example: </I> 173 parts of 1-amino-2-chloro-4-nitrobenzene are diazotized and treated with a solution of 180 parts (N-ethyl-N-phenyl) -p-amino-propionic acid -nitrile coupled in 250 parts of concentrated hydrochloric acid and 2000 parts of water with the addition of enough sodium acetate that the solution is no longer mineral acid. The coupling ends after a short time.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE181249X | 1934-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH181249A true CH181249A (en) | 1935-12-15 |
Family
ID=5715121
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH181249D CH181249A (en) | 1934-03-22 | 1935-02-06 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH181249A (en) |
-
1935
- 1935-02-06 CH CH181249D patent/CH181249A/en unknown
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